Biotech CSV Engineer: Validation, GxP & Compliance

A leading employee-owned consulting firm based in Greenville, South Carolina is seeking an experienced Computer Systems Validation Specialist. The ideal candidate will have a strong background in authoring GxP validation documentation and a solid understanding of FDA regulations. Responsibilities include collaborating with client teams for validation compliance and providing technical execution support. The role demands excellent communication skills and the ability to travel domestically and internationally. Join a team committed to integrity and excellence. #J-18808-Ljbffr